JP2008127524A - Rubber composition and pneumatic tire using the same - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a rubber composition with a drastically reduced loss tangent (tan δ) while maintaining a storage elastic modulus (G'). <P>SOLUTION: This rubber composition comprises a rubber component (A) composed of at least one among a natural rubber and a synthetic diene rubber, a low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) of a weight average molecular weight of 2,000-200,000 in terms of polystyrene measured by gel permeation chromatography, and hydrated silicic acid (C) having a cetyltrimethylammonium bromide (CTAB) adsorption specific surface area of 50-250 m<SP>2</SP>/g and satisfying a relationship of following equation (I): Y<5.00+0.47×X [wherein Y is a mass reduction% when heated at 750°C for 3 hr, and X is a mass reduction% when heated at 105°C for 2 hr]. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to a rubber composition and a pneumatic tire using the rubber composition in at least a ground contact portion of a tread portion, and particularly reduces loss tangent (tan δ) while maintaining storage elastic modulus (G ′). The present invention relates to a rubber composition.

  In recent years, there has been an increasing demand for lower fuel consumption of automobiles in connection with the movement of global carbon dioxide emission regulations due to increasing interest in environmental problems. In order to meet such demands, reduction of rolling resistance is also demanded for tire performance. Here, as a technique for reducing the rolling resistance of the tire, it is effective to use a low heat-generating rubber composition having a lower loss tangent (tan δ) as a rubber composition applied to the tread portion of the tire. As a technique for reducing the heat generation of the rubber composition, that is, a technique for reducing the loss tangent, a technique of blending silica instead of carbon black, which is widely used as a reinforcing filler for rubber, is well known. Yes.

  However, conventionally used silica is hydrous silicic acid produced mainly by a wet method, and many commercially available products are in circulation, but the particles are separated from each other by hydrogen bonding of silanol groups which are the surface functional groups. When the hydrated silicic acid is blended easily, the viscosity at the time of kneading of the rubber composition increases, and there is a problem that processability deteriorates. Moreover, since the dispersibility of the hydrous silicate particles in the rubber component becomes insufficient due to the aggregation of the hydrous silicate particles, the hysteresis loss of the resulting rubber composition tends to deteriorate and the low exothermicity tends to deteriorate. .

  On the other hand, by adding a hydrous silicic acid having less silanol groups to the rubber component to prepare a rubber composition, agglomeration of the hydrous silicic acid due to the silanol group is suppressed, and the hydrous silicic acid to the rubber component The dispersibility of the rubber composition can be improved, and the low heat build-up and the fracture resistance of the rubber composition can be improved. For example, in Japanese Patent Application Laid-Open Nos. 61-215633 and 61-215637, silica is used from 250 ° C. A technique for reducing surface silanol groups and reducing hydrogen bonds between silicas by heating at 450 ° C. is disclosed.

JP 61-215633 A JP-A-61-215637

  By the way, the rubber composition applied to the tread portion of the tire is required to have a high storage elastic modulus (G ′) in addition to the low loss tangent (tan δ) described above. On the other hand, when the present inventors examined, when a rubber composition was prepared by blending the above-mentioned hydrous silicic acid having few silanol groups, the loss tangent (tan δ) was reduced, but the hydrous silicic acid to the rubber component was reduced. It has been found that a decrease in storage elastic modulus (G ′) is unavoidable with the improvement in dispersibility.

  Therefore, an object of the present invention is to provide a rubber composition that solves the above-described problems of the prior art and that significantly reduces the loss tangent (tan δ) while maintaining the storage elastic modulus (G ′). Another object of the present invention is to provide a pneumatic tire using such a rubber composition in at least a ground contact portion of a tread portion.

  As a result of intensive studies to achieve the above object, the present inventor has a CTAB adsorption specific surface area within a specific range as a reinforcing filler, and a mass loss% (loss of ignition) when heated at 750 ° C. for 3 hours. And using hydrous silicic acid satisfying a specific relationship with the mass loss% (heat loss) when heated at 105 ° C for 2 hours, instead of softeners such as aroma oils commonly used in rubber compositions The loss tangent (tan δ) while maintaining the storage elastic modulus (G ′) of the rubber composition by using a relatively low molecular weight aromatic vinyl compound-conjugated diene compound copolymer having a specific weight average molecular weight Has been found to be significantly reduced, and the present invention has been completed.

That is, the rubber composition of the present invention is
For the rubber component (A) comprising at least one of natural rubber and synthetic diene rubber,
A low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) having a polystyrene-reduced weight average molecular weight of 2,000 to 200,000 measured by gel permeation chromatography;
Cetyltrimethylammonium bromide (CTAB) adsorption specific surface area is 50 to 250 m ² / g, and the following formula (I):
Y <5.00 + 0.47 x X (I)
Hydrous silicic acid (C) satisfying the relationship: [wherein Y is the mass loss% when heated at 750 ° C. for 3 hours, and X is the mass loss% when heated at 105 ° C. for 2 hours] It is characterized by blending.

  In the rubber composition of the present invention, the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) preferably has an aromatic vinyl compound content of 5 to 80% by mass, and the vinyl in the conjugated diene compound portion. The binding amount is preferably 5 to 80% by mass.

  In a preferred example of the rubber composition of the present invention, the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) has at least one functional group. Here, as the functional group, a tin-containing functional group, a silicon-containing functional group, and a nitrogen-containing functional group are preferable.

  In another preferred embodiment of the rubber composition of the present invention, the amount of the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) is 2 to 100 parts by mass with respect to 100 parts by mass of the rubber component (A). 60 parts by mass. Here, the total amount of the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) and the softening agent may be 2 to 80 parts by mass with respect to 100 parts by mass of the rubber component (A). preferable.

  In another preferred embodiment of the rubber composition of the present invention, the amount of the hydrous silicate (C) is 15 to 90 parts by mass with respect to 100 parts by mass of the rubber component (A).

In another preferred embodiment of the rubber composition of the present invention, the content of the aromatic vinyl compound unit in the rubber component (A) and the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) The content of the aromatic vinyl compound unit is the following formula (II):
| StA-StB | ≦ 30 (II)
[Wherein StA represents the content (% by mass) of the aromatic vinyl compound unit in the rubber component (A), and StB represents the aromatic in the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B). The content (% by mass) of the vinyl compound unit is shown]. Here, the left side of the formula (II) indicates the absolute value of the value obtained by subtracting StB from StA, that is, the difference between StA and StB.

  In another preferred embodiment of the rubber composition of the present invention, 50% by mass or more of the rubber component (A) is a styrene-butadiene copolymer rubber.

  In the rubber composition of the present invention, the aromatic vinyl compound in the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) is preferably styrene, and the low molecular weight aromatic vinyl compound-conjugated diene compound. The conjugated diene compound in the copolymer (B) is preferably 1,3-butadiene.

  In the rubber composition of the present invention, the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) preferably has a polystyrene equivalent weight average molecular weight of 20,000 to 150,000 measured by gel permeation chromatography, More preferred is ~ 100,000.

  The pneumatic tire of the present invention is characterized in that the rubber composition is used for at least a ground contact portion of a tread portion.

  According to the present invention, the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) and the hydrous silicic acid (C) are blended, and the loss is maintained while maintaining the storage elastic modulus (G ′). A rubber composition having a significantly reduced tangent (tan δ) can be provided. Further, it is possible to provide a pneumatic tire that uses such a rubber composition in at least the ground contact portion of the tread portion and has excellent steering stability and remarkably excellent fuel efficiency.

The present invention is described in detail below. The rubber composition of the present invention has a low molecular weight of 2,000 to 200,000 in terms of polystyrene equivalent weight average molecular weight measured by gel permeation chromatography with respect to a rubber component (A) comprising at least one of natural rubber and synthetic diene rubber. Hydrous silicic acid (C) having an adsorption specific surface area of 50 to 250 m ² / g and aromatic vinyl compound-conjugated diene compound copolymer (B) and cetyltrimethylammonium bromide (CTAB) satisfying the relationship of the above formula (I) ).

  Since the hydrous silicic acid (C) contained in the rubber composition of the present invention has less silanol groups than ordinary silica, hardly aggregates and has high dispersibility, it reduces the loss tangent (tan δ) of the rubber composition. Can do. However, the hydrous silicic acid (C) simultaneously decreases the storage elastic modulus (G ′) of the rubber composition. On the other hand, in place of a softening agent such as aroma oil, a low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) having a polystyrene-equivalent weight average molecular weight of 2,000 to 200,000 measured by gel permeation chromatography is used as a rubber composition. By blending, loss tangent (tan δ) can be reduced while improving storage elastic modulus (G ′) without deteriorating workability of the rubber composition. And it can maintain the storage elastic modulus (G ') of a rubber composition by using a combination of hydrous silicic acid (C) and a low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B). In addition, the loss tangent (tan δ) of the rubber composition can be greatly reduced by the synergistic effect of the hydrous silicic acid (C) and the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B). .

  The rubber component (A) of the rubber composition of the present invention comprises at least one of natural rubber (NR) and synthetic diene rubber, and the rubber component (A) is any of unmodified rubber and modified rubber. May be used. Here, as the synthetic diene rubber, those synthesized by emulsion polymerization or solution polymerization are preferable. Specific examples of the synthetic diene rubber include polyisoprene rubber (IR), styrene-butadiene copolymer rubber (SBR), polybutadiene rubber (BR), ethylene-propylene-diene rubber (EPDM), chloroprene rubber ( CR), halogenated butyl rubber, acrylonitrile-butadiene rubber (NBR) and the like. The rubber component (A) is preferably natural rubber, polyisoprene rubber, styrene-butadiene copolymer rubber, or polybutadiene rubber, and 50% by mass or more of the rubber component (A) is styrene-butadiene copolymer rubber. More preferably. When 50% by mass or more of the rubber component (A) is a styrene-butadiene copolymer rubber, an effect of suppressing a decrease in storage elastic modulus (G ′) due to the blending of the low molecular weight copolymer (B) and The effect of reducing the loss tangent (tan δ) becomes remarkable. In addition, the said rubber component (A) may be used individually by 1 type, and may blend and use 2 or more types.

  The low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) used in the rubber composition of the present invention has a polystyrene-equivalent weight average molecular weight of 2,000 to 200,000 and 20,000 to 150,000 as measured by gel permeation chromatography. It is preferably 50,000 to 100,000. If the weight average molecular weight is less than 2,000, a decrease in storage elastic modulus (G ′) of the rubber composition cannot be suppressed, while if it exceeds 200,000, the processability of the rubber composition is deteriorated.

  The amount of the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) is preferably in the range of 2 to 60 parts by mass with respect to 100 parts by mass of the rubber component (A). When the blending amount of the low molecular weight copolymer (B) is less than 2 parts by mass, the workability of the rubber composition is deteriorated. On the other hand, when it exceeds 60 parts by mass, the fracture characteristics of the vulcanized rubber tend to deteriorate.

  The low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) preferably has an aromatic vinyl compound content of 5 to 80% by mass. When the binding amount of the aromatic vinyl compound is less than 5% by mass or more than 80% by mass, the suppression of the decrease in storage elastic modulus (G ′) and the loss tangent (tan δ) of the rubber composition cannot be sufficiently achieved. There is.

  The low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) preferably has a vinyl bond content in the conjugated diene compound portion of 5 to 80% by mass. When the amount of vinyl bonds in the conjugated diene compound portion is less than 5% by mass or more than 80% by mass, it is not possible to sufficiently satisfy the suppression of the storage elastic modulus (G ′) and the loss tangent (tan δ) of the rubber composition. Sometimes.

  The low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) is obtained by copolymerizing a monomeric aromatic vinyl compound and a conjugated diene compound using a polymerization initiator, for example, It can be produced by anionic polymerization. Here, examples of the aromatic vinyl compound include styrene, p-methylstyrene, m-methylstyrene, p-tert-butylstyrene, α-methylstyrene, chloromethylstyrene, vinyltoluene and the like. Among these, styrene Is preferred. On the other hand, examples of the conjugated diene compound include 1,3-butadiene, isoprene, 1,3-pentadiene, 2,3-dimethylbutadiene, and among these, 1,3-butadiene is preferable. As the polymerization initiator, an organic alkali metal compound described later can be used.

  The low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) preferably has at least one functional group, and examples of the functional group include a tin-containing functional group, a silicon-containing functional group, and a nitrogen-containing functional group. Is preferred. By blending the low molecular weight copolymer (B) having a functional group into the rubber composition, the loss tangent can be significantly reduced while maintaining the storage elastic modulus at a high temperature. The low molecular weight copolymer (B) having a functional group is obtained by (1) copolymerizing an aromatic vinyl compound as a monomer and a conjugated diene compound using a polymerization initiator, and having an polymerization active site. A method in which a compound-conjugated diene compound copolymer is produced and then the polymerization active site is modified with various modifiers, or (2) a monomer having an aromatic vinyl compound and a conjugated diene compound having a functional group It can be obtained by a method of copolymerization using a polymerization initiator. Here, the aromatic vinyl compound-conjugated diene compound copolymer having a polymerization active site can be produced, for example, by anionic polymerization.

  When producing an aromatic vinyl compound-conjugated diene compound copolymer having a polymerization active site by anionic polymerization, an organic alkali metal compound is preferably used as a polymerization initiator, and a lithium compound is more preferably used. Examples of the lithium compound include hydrocarbyl lithium and lithium amide compounds. When hydrocarbyl lithium is used as the polymerization initiator, a copolymer having a hydrocarbyl group at the polymerization initiation terminal and the other terminal being a polymerization active site is obtained. On the other hand, when a lithium amide compound is used as a polymerization initiator, a copolymer having a nitrogen-containing functional group at the polymerization start terminal and the other terminal being a polymerization active site is obtained, and the copolymer is a modifier. Further, it may be modified or not. The amount of the organic alkali metal compound used as the polymerization initiator is preferably in the range of 0.2 to 20 mmol per 100 g of monomer.

  Examples of the hydrocarbyl lithium include ethyl lithium, n-propyl lithium, isopropyl lithium, n-butyl lithium, sec-butyl lithium, tert-octyl lithium, n-decyl lithium, phenyl lithium, 2-naphthyl lithium, and 2-butyl-phenyl. Examples include lithium, 4-phenyl-butyllithium, cyclohexyllithium, cyclopentyllithium, reaction products of diisopropenylbenzene and butyllithium, and among these, ethyllithium, n-propyllithium, isopropyllithium, n-butyl Alkyl lithium such as lithium, sec-butyl lithium, tert-octyl lithium and n-decyl lithium is preferable, and n-butyl lithium is particularly preferable.

  On the other hand, the lithium amide compounds include lithium hexamethylene imide, lithium pyrrolidide, lithium piperidide, lithium heptamethylene imide, lithium dodecamethylene imide, lithium dimethylamide, lithium diethylamide, lithium dipropylamide, lithium dibutylamide, lithium Dihexylamide, lithium diheptylamide, lithium dioctylamide, lythym-2-ethylhexylamide, lithium didecylamide, lithium-N-methylpiperazide, lithium ethylpropylamide, lithium ethylbutyramide, lithium methylbutyramide, lithium ethylbenzylamide, Examples include lithium methylphenethyl amide, among these, lithium hexamethylene imide, lithium pyrrolidide, lithium Cyclic lithium amide compounds such as piperidide, lithium heptamethylene imide and lithium dodecamethylene imide are preferred, and lithium hexamethylene imide and lithium pyrrolidide are particularly preferred.

（式中、Ｒ¹は、それぞれ独立して炭素数１〜１２のアルキル基、シクロアルキル基又はアラルキル基である）で表される置換アミノ基又は下記式(IV)：

（式中、Ｒ²は、３〜１６のメチレン基を有するアルキレン基、置換アルキレン基、オキシアルキレン基又はＮ-アルキルアミノ-アルキレン基を示す）で表される環状アミノ基である］で表されるリチウムアミド化合物を用いることで、式(III)で表される置換アミノ基及び式(IV)で表される環状アミノ基からなる群から選択される少なくとも一種の窒素含有官能基が導入された低分子量共重合体（Ｂ）が得られる。 As the lithium amide compound, the formula: Li-AM [wherein AM represents the following formula (III):

(Wherein R ¹ is each independently an alkyl group having 1 to 12 carbon atoms, a cycloalkyl group, or an aralkyl group) or a substituted amino group represented by the following formula (IV):

Wherein R ² is a cyclic amino group represented by an alkylene group having 3 to 16 methylene groups, a substituted alkylene group, an oxyalkylene group or an N-alkylamino-alkylene group. By using the lithium amide compound, at least one nitrogen-containing functional group selected from the group consisting of a substituted amino group represented by the formula (III) and a cyclic amino group represented by the formula (IV) was introduced. A low molecular weight copolymer (B) is obtained.

In the formula (III), R ¹ is an alkyl group having 1 to 12 carbon atoms, a cycloalkyl group or an aralkyl group, and specifically includes a methyl group, an ethyl group, a butyl group, an octyl group, a cyclohexyl group, a 3- Preferable examples include phenyl-1-propyl group and isobutyl group. R ¹ may be the same or different.

In the formula (IV), R ² is an alkylene group having 3 to 16 methylene groups, a substituted alkylene group, an oxyalkylene group or an N-alkylamino-alkylene group. Here, the substituted alkylene group includes a mono- to octa-substituted alkylene group, and examples of the substituent include a linear or branched alkyl group having 1 to 12 carbon atoms, a cycloalkyl group, a bicycloalkyl group, and an aryl group. Groups and aralkyl groups. R ² is specifically preferably a trimethylene group, a tetramethylene group, a hexamethylene group, an oxydiethylene group, an N-alkylazadiethylene group, a dodecamethylene group, a hexadecamethylene group, or the like.

  The lithium amide compound may be preliminarily prepared from a secondary amine and a lithium compound and used for the polymerization reaction, but may be generated in a polymerization system. Here, examples of the secondary amine include dimethylamine, diethylamine, dibutylamine, dioctylamine, dicyclohexylamine, diisobutylamine and the like, as well as azacycloheptane (ie, hexamethyleneimine), 2- (2-ethylhexyl) pyrrolidine, 3 -(2-propyl) pyrrolidine, 3,5-bis (2-ethylhexyl) piperidine, 4-phenylpiperidine, 7-decyl-1-azacyclotridecane, 3,3-dimethyl-1-azacyclotetradecane, 4- Dodecyl-1-azacyclooctane, 4- (2-phenylbutyl) -1-azacyclooctane, 3-ethyl-5-cyclohexyl-1-azacycloheptane, 4-hexyl-1-azacycloheptane, 9-isoamyl -1-Azacycloheptadecane, 2-methyl-1-azacycloheptadec-9-ene, 3-isobutyl-1-azacyclododecane 2-Methyl-7-tert-butyl-1-azacyclododecane, 5-nonyl-1-azacyclododecane, 8- (4′-methylphenyl) -5-pentyl-3-azabicyclo [5.4.0] ] Undecane, 1-butyl-6-azabicyclo [3.2.1] octane, 8-ethyl-3-azabicyclo [3.2.1] octane, 1-propyl-3-azabicyclo [3.2.2] nonane And cyclic amines such as 3- (t-butyl) -7-azabicyclo [4.3.0] nonane and 1,5,5-trimethyl-3-azabicyclo [4.4.0] decane. On the other hand, as the lithium compound, the above hydrocarbyl lithium can be used.

  The method for producing the low molecular weight copolymer (B) by the anionic polymerization is not particularly limited. For example, in a hydrocarbon solvent inert to the polymerization reaction, a mixture of a conjugated diene compound and an aromatic vinyl compound is used. A copolymer can be produced by polymerization. Here, hydrocarbon solvents inert to the polymerization reaction include propane, n-butane, isobutane, n-pentane, isopentane, n-hexane, cyclohexane, propene, 1-butene, isobutene, trans-2-butene, cis -2-butene, 1-pentene, 2-pentene, 1-hexene, 2-hexene, benzene, toluene, xylene, ethylbenzene and the like.

  The anionic polymerization may be performed in the presence of a randomizer. The randomizer can control the microstructure of the conjugated diene compound portion of the copolymer. More specifically, the randomizer can control the vinyl bond amount of the conjugated diene compound portion of the copolymer, The conjugated diene compound unit and the aromatic vinyl compound unit are randomized. Examples of the randomizer include dimethoxybenzene, tetrahydrofuran, dimethoxyethane, diethylene glycol dibutyl ether, diethylene glycol dimethyl ether, bistetrahydrofurylpropane, triethylamine, pyridine, N-methylmorpholine, N, N, N ′, N′-tetramethylethylenediamine, 1 , 2-dipiperidinoethane, potassium-t-amylate, potassium-t-butoxide, sodium-t-amylate and the like. The amount of these randomizers used is preferably in the range of 0.01 to 100 molar equivalents per mole of polymerization initiator.

  The anionic polymerization is preferably carried out by solution polymerization, and the concentration of the monomer in the polymerization reaction solution is preferably in the range of 5 to 50% by mass, more preferably in the range of 10 to 30% by mass. The content of the aromatic vinyl compound in the mixture of the conjugated diene compound and the aromatic vinyl compound is preferably in the range of 5 to 80% by mass, and the amount of the aromatic vinyl compound in the target copolymer (B) is as follows. It can be appropriately selected depending on the case. Further, the polymerization mode is not particularly limited, and may be batch type or continuous type.

  The polymerization temperature of the anionic polymerization is preferably in the range of 0 to 150 ° C, more preferably in the range of 20 to 130 ° C. The polymerization can be carried out under a generated pressure, but it is usually preferred to carry out the polymerization under a pressure sufficient to keep the monomer used in a substantially liquid phase. Here, when the polymerization reaction is carried out under a pressure higher than the generated pressure, it is preferable to pressurize the reaction system with an inert gas. Moreover, it is preferable to use what removed reaction-inhibiting substances, such as water, oxygen, a carbon dioxide, and a protic compound, as raw materials, such as a monomer used for superposition | polymerization, a polymerization initiator, and a solvent.

  In modifying the polymerization active site of the copolymer having a polymerization active site with a modifier, the modifier used is preferably a nitrogen-containing compound, a silicon-containing compound or a tin-containing compound. In this case, a nitrogen-containing functional group, a silicon-containing functional group, or a tin-containing functional group can be introduced by a modification reaction.

  The nitrogen-containing compound that can be used as the modifier preferably has a substituted or unsubstituted amino group, amide group, imino group, imidazole group, nitrile group, or pyridyl group. Suitable nitrogen-containing compounds as the modifier include isocyanate compounds such as diphenylmethane diisocyanate, crude MDI, trimethylhexamethylene diisocyanate, tolylene diisocyanate, 4- (dimethylamino) benzophenone, 4- (diethylamino) benzophenone, 4-dimethylamino. Examples include benzylideneaniline, 4-dimethylaminobenzylidenebutylamine, dimethylimidazolidinone, N-methylpyrrolidone and the like.

［式中、Ａは(チオ)エポキシ、(チオ)インシアネート、(チオ)ケトン、(チオ)アルデヒド、イミン、アミド、イソシアヌル酸トリエステル、(チオ)カルボン酸ヒドロカルビルエステル、(チオ)カルボン酸の金属塩、カルボン酸無水物、カルボン酸ハロゲン化物、炭酸ジヒドロカルビルエステル、環状三級アミン、非環状三級アミン、ニトリル、ピリジン、スルフィド及びマルチスルフィドの中から選ばれる少なくとも一種の官能基を有する一価の基で；Ｒ³は単結合又は二価の不活性炭化水素基で；Ｒ⁴及びＲ⁵は、それぞれ独立に炭素数１〜２０の一価の脂肪族炭化水素基又は炭素数６〜１８の一価の芳香族炭化水素基で；ｎは０〜２の整数であり；ＯＲ⁵が複数ある場合、複数のＯＲ⁵はたがいに同一でも異なっていてもよく；また分子中には活性プロトン及びオニウム塩は含まれない］で表されるヒドロカルビルオキシシラン化合物及びその部分縮合物、並びに、下記式(VI)：
Ｒ⁶ _p−Ｓｉ−(ＯＲ⁷)_4-p ・・・ (VI)
［式中、Ｒ⁶及びＲ⁷は、それぞれ独立して炭素数１〜２０の一価の脂肪族炭化水素基又は炭素数６〜１８の一価の芳香族炭化水素基であり；ｐは０〜２の整数であり；ＯＲ⁷が複数ある場合、複数のＯＲ⁷はたがいに同一でも異なっていてもよく；また分子中には活性プロトン及びオニウム塩は含まれない］で表されるヒドロカルビルオキシシラン化合物及びその部分縮物も好ましい。 Examples of the silicon-containing compound that can be used as the modifier include the following formula (V):

[Wherein A represents (thio) epoxy, (thio) inocyanate, (thio) ketone, (thio) aldehyde, imine, amide, isocyanuric acid triester, (thio) carboxylic acid hydrocarbyl ester, (thio) carboxylic acid One having at least one functional group selected from metal salts, carboxylic acid anhydrides, carboxylic acid halides, carbonic acid dihydrocarbyl esters, cyclic tertiary amines, acyclic tertiary amines, nitriles, pyridines, sulfides and multisulfides. R ³ is a single bond or a divalent inert hydrocarbon group; R ⁴ and R ⁵ are each independently a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms or 6 to 6 carbon atoms. 18 monovalent aromatic hydrocarbon group; n is an integer from 0 to 2; if OR ⁵ have multiple or different and a plurality of OR ⁵ is identical to each other; in addition the molecule active And a partial condensate thereof, and the following formula (VI):
R ⁶ _p -Si- (OR ⁷ ) _4-p (VI)
[Wherein, R ⁶ and R ⁷ are each independently a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms or a monovalent aromatic hydrocarbon group having 6 to 18 carbon atoms; It is ~ 2 integer; If oR ⁷ there are a plurality, a plurality of oR ⁷ each other may be the same or different; hydrocarbyloxy represented by not included active proton and onium salt are also in the molecule] Silane compounds and partial condensates thereof are also preferred.

  In formula (V), among the functional groups in A, imine includes ketimine, aldimine, and amidine, (thio) carboxylic acid ester includes unsaturated carboxylic acid ester such as acrylate and methacrylate, Secondary amines include N, N-disubstituted aromatic amines such as N, N-disubstituted anilines, and cyclic tertiary amines can include (thio) ethers as part of the ring. Examples of the metal of the metal salt of (thio) carboxylic acid include alkali metals, alkaline earth metals, Al, Sn, and Zn.

The divalent inert hydrocarbon group in R ³ is preferably an alkylene group having 1 to 20 carbon atoms. The alkylene group may be linear, branched or cyclic, but is particularly preferably linear. Examples of the linear alkylene group include a methylene group, an ethylene group, a trimethylene group, a tetramethylene group, a pentamethylene group, a hexamethylene group, an octamethylene group, a decamethylene group, and a dodecamethylene group.

Examples of R ⁴ and R ⁵ include an alkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 18 carbon atoms, an aryl group having 6 to 18 carbon atoms, and an aralkyl group having 7 to 18 carbon atoms. Here, the alkyl group and alkenyl group may be linear, branched, or cyclic, for example, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl, tert-butyl, pentyl, hexyl, octyl, decyl, dodecyl, cyclopentyl, cyclohexyl, vinyl, propenyl, allyl, hexenyl, octenyl, cyclopentenyl Group, cyclohexenyl group and the like. The aryl group may have a substituent such as a lower alkyl group on the aromatic ring, and examples thereof include a phenyl group, a tolyl group, a xylyl group, and a naphthyl group. Furthermore, the aralkyl group may have a substituent such as a lower alkyl group on the aromatic ring, and examples thereof include a benzyl group, a phenethyl group, and a naphthylmethyl group.

  In the formula (V), n is an integer of 0 to 2, but 0 is preferable, and it is necessary that this molecule does not have active protons and onium salts.

  Examples of the hydrocarbyloxysilane compound represented by the formula (V) include 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, N- (1-methylpropylidene) -3- (triethoxy Silyl) -1-propanamine, N- (1,3-dimethylbutylidene) -3- (triethoxysilyl) -1-propanamine, N- (3-triethoxysilylpropyl) -4,5-dihydroimidazole 3-methacryloyloxypropyltrimethoxysilane, 3-isocyanatopropyltriethoxysilane, 3-triethoxysilylpropyl succinic anhydride, 3- (1-hexamethyleneimino) propyl (triethoxy) silane, (1-hexa Methyleneimino) methyl (trimethoxy) silane, 3-diethylaminopropyl (triethoxy) silane, 3-dimethylaminopropyl (triethoxy) Run, 2- (trimethoxysilyl ethyl) pyridine, 2- (triethoxysilylethyl) pyridine, 2-cyanoethyl triethoxy silane and the like.

In formula (VI), R ⁶ and R ⁷ are as described for R ⁴ and R ⁵ in formula (V), respectively. Examples of the hydrocarbyloxysilane compound represented by the formula (VI) include tetramethoxysilane, tetraethoxysilane, tetra-n-propoxysilane, tetraisopropoxysilane, tetra-n-butoxysilane, and tetraisobutoxysilane. , Tetra-sec-butoxysilane, tetra-tert-butoxysilane, methyltrimethoxysilane, methyltriethoxysilane, methyltripropoxysilane, methyltriisopropoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, propyltriethoxysilane , Butyltrimethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, dimethyldimethoxysilane, methylphenyldimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, divinyldi Examples include methoxysilane and divinyldiethoxysilane. Among these, tetraethoxysilane is particularly preferable.

  The hydrocarbyloxysilane compounds of the above formulas (V) and (VI) may be used singly or in combination of two or more. Moreover, the partial condensate of these hydrocarbyl oxysilane compounds can also be used.

Examples of the modifying agent include the following formula (VII):
R ⁸ _a ZX _b ... (VII)
[Wherein, R ⁸ each independently comprises an alkyl group having 1 to 20 carbon atoms, a cycloalkyl group having 3 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, and an aralkyl group having 7 to 20 carbon atoms. Selected from the group; Z is tin or silicon; X is each independently chlorine or bromine; a is 0-3, b is 1-4, provided that a + b = 4. The coupling agent represented is also preferred. By modifying with the coupling agent of the formula (VII), the cold flow resistance of the copolymer (B) can be improved. The copolymer (B) obtained by modifying with a coupling agent of the formula (VII) has at least one tin-carbon bond or silicon-carbon bond. Specific examples of R ^{8 in the} formula (VII) include a methyl group, an ethyl group, an n-butyl group, a neophyll group, a cyclohexyl group, an n-octyl group, and a 2-ethylhexyl group. Specific examples of the coupling agent of the formula (VII) include SnCl ₄ , R ⁸ SnCl ₃ , R ⁸ ₂ SnCl ₂ , R ⁸ ₃ SnCl, SiCl ₄ , R ⁸ SiCl ₃ , R ⁸ ₂ SiCl ₂ , R ⁸ ₃ SiCl and the like are preferable, and SnCl ₄ and SiCl ₄ are particularly preferable.

  The modification reaction of the polymerization active site by the modifying agent is preferably performed by a solution reaction, and the solution may contain a monomer used at the time of polymerization. The reaction mode of the modification reaction is not particularly limited, and may be a batch type or a continuous type. Furthermore, the reaction temperature of the modification reaction is not particularly limited as long as the reaction proceeds, and the reaction temperature of the polymerization reaction may be employed as it is. The amount of modifier used is preferably in the range of 0.25 to 3.0 mol, and more preferably in the range of 0.5 to 1.5 mol, with respect to 1 mol of the polymerization initiator used for the production of the copolymer.

The content of the aromatic vinyl compound unit in the rubber component (A) and the content of the aromatic vinyl compound unit in the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) are represented by the following formula ( II):
| StA-StB | ≦ 30 (II)
[Wherein StA represents the content (% by mass) of the aromatic vinyl compound unit in the rubber component (A), and StB represents the aromatic in the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B). It is preferable that the relationship of the content (% by mass) of the vinyl compound unit is satisfied. When the rubber component (A) and the low molecular weight copolymer (B) do not satisfy the relationship of the above formula (II), that is, the aromatic vinyl compound unit of the rubber component (A) and the low molecular weight copolymer (B). When the difference in content exceeds 30% by mass, the compatibility between the rubber component (A) and the low molecular weight copolymer (B) may be deteriorated, and the physical properties of the vulcanized rubber may be lowered. Here, from the viewpoint of improving the compatibility between the rubber component (A) and the low molecular weight copolymer (B), the content of the aromatic vinyl compound unit in the rubber component (A) and the low molecular weight copolymer (B). The difference is more preferably 20% by mass or less, and further preferably 15% by mass or less.

The hydrous silicic acid (C) used in the rubber composition of the present invention has a cetyltrimethylammonium bromide (CTAB) adsorption specific surface area of 50 to 250 m ² / g, preferably 80 to 240 m ² / g. When the CTAB adsorption specific surface area of the hydrous silicic acid (C) is less than 50 m ² / g, the storage elastic modulus of the rubber composition decreases. On the other hand, when it exceeds 250 m ² / g, the viscosity of the rubber composition when unvulcanized As a result, the processability deteriorates. Moreover, when the CTAB adsorption specific surface area of the said hydrous silicic acid (C) is 80-240 m < ² > / g, the loss tangent of a rubber composition can further be reduced.

The hydrous silicic acid (C) is represented by the following formula (I):
Y <5.00 + 0.47 x X (I)
In the formula, Y is the mass loss% when heated at 750 ° C. for 3 hours, and X is the mass loss% when heated at 105 ° C. for 2 hours. In formula (I), the mass loss when heated at 105 ° C for 2 hours is due to the desorption of water physically adsorbed on hydrous silicic acid (C), while the mass loss when heated at 750 ° C for 3 hours Is caused by (C) desorption of water physically adsorbed to hydrous silicic acid and disappearance of silanol groups of hydrous silicic acid (C). The hydrous silicic acid (C) satisfying the relationship of the above formula (I) has less silanol groups and is therefore less likely to agglomerate than ordinary silica and can reduce the loss tangent (tan δ) of the rubber composition.

  The hydrous silicic acid (C) can be produced by adjusting various conditions when producing the hydrous silicic acid by a wet method, and the hydrous silicic acid (C) is subjected to silicone treatment. Hydrophobic silica, heat-treated silica and the like can also be used. In the rubber composition of the present invention, the amount of the hydrous silicic acid (C) is not particularly limited, but is preferably in the range of 10 to 150 parts by mass with respect to 100 parts by mass of the rubber component (A). The range of 15 to 90 parts by mass is more preferable. If the amount of hydrous silicic acid is less than 10 parts by mass, the reinforcing property of the rubber composition may be insufficient. On the other hand, if it exceeds 150 parts by mass, the processability of the rubber composition may be deteriorated. Moreover, if the compounding quantity of a hydrous silicic acid is the range of 15-90 mass parts, the loss tangent of a rubber composition can be reduced significantly, ensuring the reinforcement property and workability of a rubber composition.

  The rubber composition of the present invention may further contain a softening agent. Here, examples of the softener include process oils such as paraffin oil, naphthenic oil, and aroma oil. The blending amount of the softening agent is not particularly limited, but the total blending amount of the low molecular weight copolymer (B) and the softening agent is 2 to 80 with respect to 100 parts by mass of the rubber component (A). It is preferable to mix | blend so that it may become a mass part. When the total amount of the low molecular weight copolymer (B) and the softening agent exceeds 80 parts by mass, the fracture characteristics of the vulcanized rubber tend to be lowered.

  In the rubber composition of the present invention, in addition to the rubber component (A), the low molecular weight copolymer (B), the hydrous silicic acid (C), the softening agent, a compounding agent usually used in the rubber industry, for example, In addition, a filler such as carbon black, an anti-aging agent, a silane coupling agent, a vulcanization accelerator, a vulcanization accelerator, a vulcanizer, and the like are appropriately selected and blended within a range that does not impair the object of the present invention. be able to. As these compounding agents, commercially available products can be suitably used. The rubber composition is blended with the rubber component (A) by blending a low molecular weight copolymer (B) and hydrous silicic acid (C) and various compounding agents appropriately selected as necessary, and kneading. It can be produced by hot-pressing, extruding or the like.

  The pneumatic tire of the present invention is characterized in that the rubber composition is used in at least a ground contact portion of a tread portion. A tire using the rubber composition in at least the ground contact portion of the tread portion has good steering stability and excellent fuel efficiency. The pneumatic tire of the present invention is not particularly limited except that the above rubber composition is used for at least the ground contact portion of the tread portion, and can be produced according to a conventional method. Moreover, as gas with which this tire is filled, inert gas, such as nitrogen, argon, helium other than normal or the air which adjusted oxygen partial pressure, can be used.

  Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to the following examples.

<Production Example 1 of Hydrous Silicic Acid>
A 180 L jacketed stainless steel reactor equipped with a stirrer was charged with 93 L of water and 0.6 L of a sodium silicate aqueous solution (SiO ₂ 160 g / L, SiO ₂ / Na ₂ O molar ratio 3.3) and heated to 96 ° C. The concentration of Na ₂ O in the resulting solution was 0.005 mol / L. While maintaining the temperature of this solution at 96 ° C., the same sodium silicate aqueous solution as described above was simultaneously added dropwise at a flow rate of 540 mL / min and sulfuric acid (18 mol / L) at a flow rate of 24 mL / min. The neutralization reaction was carried out while adjusting the flow rate and maintaining the Na ₂ O concentration in the reaction solution in the range of 0.00 to 0.01 mol / L. From the middle of the reaction, the reaction solution started to become cloudy, and the viscosity increased to a gel solution at 47 minutes. Further, the addition was continued and the reaction was stopped in 75 minutes. The silica concentration in the resulting solution was 49 g / L. Subsequently, sulfuric acid similar to that described above was added to finish the acidification by setting the pH of the solution to 3 to obtain a silicic acid slurry. The obtained silicic acid slurry is filtered with a filter press and washed with water to obtain a wet cake. Then, the wet cake is made into a slurry using an emulsifier and dried with a spray dryer to obtain a wet method hydrous silicic acid A. Obtained.

<Evaluation of hydrous silicic acid>
The CTAB adsorption specific surface area, heating loss and ignition loss of the hydrous silicic acid produced as described above were evaluated by the following methods. For comparison, hydrous silicic acid “Nipsil AQ” (trade name) manufactured by Tosoh Silica Co., Ltd. was also evaluated. The results are shown in Table 1.

(1) Measurement of CTAB adsorption specific surface area It was carried out according to the method described in ASTM D3765-92. However, since the method described in ASTM D3765-92 is a method for measuring CTAB of carbon black, it is a method with some improvements. In other words, a standard cetyltrimethylammonium bromide (CTAB) standard solution was prepared without using IRB # 3 (83.0 m ² / g), which is a standard product of carbon black, and thereby hydrous silicic acid OT (di-2-ethylhexyl). (Sodium sulfosuccinate) solution was standardized, and the specific surface area was calculated from the amount of CTAB adsorbed with the adsorption cross-sectional area per molecule of CTAB on the hydrous silicate surface being 0.35 nm ² . This is because carbon black and hydrous silicic acid have different surfaces, and it is considered that there is a difference in the amount of CTAB adsorbed even with the same surface area.

(2) Heat loss X and ignition loss Y
Weigh a sample of hydrous silicic acid. In the case of heating loss X, the sample is heated at 105 ° C for 2 hours. In the case of ignition loss Y, the sample is heated at 750 ° C for 3 hours, and then the sample mass is measured and heated. The difference from the previous sample mass was defined as mass reduction%.

<Production method of copolymer (B-1)>
Add 800 g of cyclohexane, 40 g of 1,3-butadiene, 13 g of styrene, 0.90 mmol of ditetrahydrofurylpropane, and 0.90 mmol of n-butyllithium (n-BuLi) to an 800 mL pressure-resistant glass container that has been dried and purged with nitrogen. After the addition, a polymerization reaction was carried out at 50 ° C. for 2 hours. The polymerization conversion rate at this time was almost 100%. Thereafter, 0.5 mL of an isopropanol solution (BHT concentration: 5% by mass) of 2,6-di-t-butyl-p-cresol (BHT) was added to the polymerization reaction system to stop the polymerization reaction, and further according to a conventional method. It dried and the copolymer (B-1) was obtained.

<Method for Producing Copolymers (B-2) to (B-3) and (B-5) to (B-10)>
Add 800 g of cyclohexane, 40 g of 1,3-butadiene, 13 g of styrene, 0.90 mmol of ditetrahydrofurylpropane, and 0.90 mmol of n-butyllithium (n-BuLi) to an 800 mL pressure-resistant glass container that has been dried and purged with nitrogen. After the addition, a polymerization reaction was carried out at 50 ° C. for 2 hours. The polymerization conversion rate at this time was almost 100%. Next, the modifiers shown in Tables 2 to 4 were quickly added to the polymerization reaction system in the amounts shown in Tables 2 to 4, and the modification reaction was further performed at 50 ° C. for 30 minutes. Thereafter, 0.5 mL of an isopropanol solution (BHT concentration: 5% by mass) of 2,6-di-t-butyl-p-cresol (BHT) was added to the polymerization reaction system to stop the polymerization reaction, and further according to a conventional method. After drying, the copolymers (B-2), (B-3), (B-5), (B-6), (B-7), (B-8), (B-9), (B -10) was obtained.

<Production method of copolymer (B-4)>
In place of n-butyllithium (n-BuLi), lithium hexamethyleneimide [HMI-Li; hexamethyleneimine (HMI) / lithium (Li) molar ratio = 0.9] prepared in situ was used as the polymerization initiator. A copolymer (B-4) was obtained in the same manner as the copolymer (B-1) except that 0.90 mmol was used in an equivalent amount.

<Method for Producing Copolymers (B-11) and (B-12)>
In place of n-butyllithium (n-BuLi), lithium hexamethyleneimide [HMI-Li; hexamethyleneimine (HMI) / lithium (Li) molar ratio = 0.9] prepared in situ was used as the polymerization initiator. Copolymers (B-11) and (B-12) were obtained in the same manner as the copolymers (B-7) and (B-5) except that 0.90 mmol was used in an equivalent amount.

  The weight average molecular weight (Mw), microstructure, and bound styrene content of the copolymers (B-1) to (B-12) produced as described above were measured by the following methods. The results are shown in Tables 2-4.

(3) Weight average molecular weight (Mw)
Gel permeation chromatography [GPC: Tosoh HLC-8020, column: Tosoh GMH-XL (two in series), detector: differential refractometer (RI)], based on monodisperse polystyrene, The weight average molecular weight (Mw) in terms of polystyrene was determined.

(4) Microstructure and amount of bound styrene The microstructure of the polymer was determined by an infrared method (Morero method), and the amount of bound styrene of the polymer was determined from the integral ratio of the ¹ H-NMR spectrum.

* 1 Tetraethoxysilane.
* 2 N- (1,3-Dimethylbutylidene) -3- (triethoxysilyl) -1-propanamine.
* 3 Crude MDI, MR400 made by Nippon Polyurethane.
* 4 N, N'-diethylaminobenzophenone.
* 5 Dimethylimidazolidinone.
* 6 N-methylpyrrolidone.
* 7 4-Dimethylaminobenzylideneaniline.
* 8 4-Dimethylaminobenzylidenebutylamine.

  Next, using the above-mentioned hydrous silicate A or “Nipsil AQ” and the above-mentioned copolymers (B-1) to (B-12) or aroma oil, a rubber composition having a formulation shown in Table 5 is prepared, Further, the rubber composition was vulcanized at 160 ° C. for 15 minutes to obtain a vulcanized rubber, and the storage elastic modulus (G ′) and loss tangent (tan δ) of the vulcanized rubber were measured by the following methods. The results are shown in Tables 6-7.

(5) Storage elastic modulus (G ′) and loss tangent (tan δ)
The storage elastic modulus (G ′) and loss tangent (tan δ) were measured at a temperature of 50 ° C., a frequency of 15 Hz, and a strain of 5% using a viscoelasticity measuring device manufactured by Rheometrics. The storage modulus and loss tangent of the composition were indexed as 100, and in Table 7, the storage modulus and loss tangent of the rubber composition of Comparative Example 3 were indexed as 100. As for the storage elastic modulus (G ′), the larger the index value, the higher the storage elastic modulus. On the other hand, as for the loss tangent (tan δ), the smaller the index value, the lower the loss tangent and the lower the heat generation. Shows superiority.

* 9 “# 1500” manufactured by JSR, bound styrene content = 24% by mass
* 10 Tokai Carbon Co., Ltd. Trademark: Seast KH (N339)
* 11 The types of silica used are shown in Tables 6 and 7.
* 12 Degussa, trademark Si69, bis (3-triethoxysilylpropyl) tetrasulfide
* 13 Tables 6 and 7 show the types of aromai oil or low molecular weight copolymer (B) used.
* 14 N- (1,3-Dimethylbutyl) -N'-phenyl-p-phenylenediamine
* 15 Diphenylguanidine.
* 16 Dibenzothiazyl disulfide.
* 17 Nt-Butyl-2-benzothiazylsulfenamide.

  From comparison between Comparative Examples 1 and 2 and Comparative Examples 3 and 4, it can be seen that replacing Nipsil AQ with hydrous silicic acid A reduces the loss tangent but also reduces the storage modulus.

  On the other hand, from the results of the examples, while using hydrous silicate A, by replacing the aroma oil with the low molecular weight copolymer (B), the loss tangent is further reduced, and the storage elastic modulus is a comparative example. It can be seen that it can be restored to levels 1 and 3.

Claims (15)

For the rubber component (A) comprising at least one of natural rubber and synthetic diene rubber,
A low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) having a polystyrene-reduced weight average molecular weight of 2,000 to 200,000 measured by gel permeation chromatography;
Cetyltrimethylammonium bromide (CTAB) adsorption specific surface area is 50 to 250 m ² / g, and the following formula (I):
Y <5.00 + 0.47 x X (I)
Hydrous silicic acid (C) satisfying the relationship: [wherein Y is the mass loss% when heated at 750 ° C. for 3 hours, and X is the mass loss% when heated at 105 ° C. for 2 hours] A rubber composition characterized by being compounded.   The rubber composition according to claim 1, wherein the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) has an aromatic vinyl compound content of 5 to 80% by mass.   2. The rubber composition according to claim 1, wherein the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) has a vinyl bond content in the conjugated diene compound portion of 5 to 80 mass%.   The rubber composition according to claim 1, wherein the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) has at least one functional group.   The rubber composition according to claim 4, wherein the functional group is a tin-containing functional group, a silicon-containing functional group, or a nitrogen-containing functional group.   The amount of the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) is 2 to 60 parts by mass with respect to 100 parts by mass of the rubber component (A). The rubber composition as described.   The total amount of the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) and the softening agent is 2 to 80 parts by mass with respect to 100 parts by mass of the rubber component (A). The rubber composition according to claim 6.   2. The rubber composition according to claim 1, wherein the amount of the hydrous silicate (C) is 15 to 90 parts by mass with respect to 100 parts by mass of the rubber component (A). The content of the aromatic vinyl compound unit in the rubber component (A) and the content of the aromatic vinyl compound unit in the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) are represented by the following formula (II ):
| StA-StB | ≦ 30 (II)
[Wherein StA represents the content (% by mass) of the aromatic vinyl compound unit in the rubber component (A), and StB represents the aromatic in the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B). The rubber composition according to claim 1, wherein the relationship of the vinyl compound unit content (% by mass) is satisfied.   The rubber composition according to claim 1, wherein 50% by mass or more of the rubber component (A) is a styrene-butadiene copolymer rubber.   The rubber composition according to claim 1, wherein the aromatic vinyl compound in the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) is styrene.   The rubber composition according to claim 1, wherein the conjugated diene compound in the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) is 1,3-butadiene.   The rubber composition according to claim 1, wherein the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) has a polystyrene-reduced weight average molecular weight of 20,000 to 150,000 as measured by gel permeation chromatography. object.   The rubber composition according to claim 13, wherein the low molecular weight aromatic vinyl compound-conjugated diene compound copolymer (B) has a polystyrene-reduced weight average molecular weight measured by gel permeation chromatography of 50,000 to 100,000. object.   A pneumatic tire using the rubber composition according to any one of claims 1 to 14 in at least a ground contact portion of a tread portion.